Canonical Allele Identifier: CA1729340649

Gene: MCM7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100098577_100098579delinsCAT , CM000669.2:g.100098577_100098579delinsCAT	GRCh38
NC_000007.13:g.99696200_99696202delinsCAT , CM000669.1:g.99696200_99696202delinsCAT	GRCh37
NC_000007.12:g.99534136_99534138delinsCAT	NCBI36
NG_016312.1:g.2071_2073delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425308.6:c.398_399+1delinsATG
ENST00000485286.6:n.1331_1332+1delinsATG
ENST00000489841.6:n.1440_1441+1delinsATG
ENST00000710813.1:c.398_399+1delinsATG
ENST00000710814.1:c.398_399+1delinsATG
ENST00000710815.1:c.398_399+1delinsATG
ENST00000303887.10:c.719_720+1delinsATG
ENST00000303887.9:c.719_720+1delinsATG
ENST00000343023.10:c.719_720+1delinsATG
ENST00000354230.7:c.191_192+1delinsATG
ENST00000425308.5:c.398_399+1delinsATG
ENST00000463722.5:n.1094_1095+1delinsATG
ENST00000485286.5:n.1308_1309+1delinsATG
ENST00000489841.5:n.870_871+1delinsATG
ENST00000491245.6:c.85+1074_85+1076delinsATG
ENST00000621318.4:c.191_192+1delinsATG
NM_001278595.1:c.191_192+1delinsATG
NM_005916.4:c.719_720+1delinsATG
NM_182776.2:c.191_192+1delinsATG
XM_005250348.2:c.398_399+1delinsATG
XM_005250348.3:c.398_399+1delinsATG
XM_017012217.2:c.398_399+1delinsATG
NM_001278595.2:c.191_192+1delinsATG
NM_005916.5:c.719_720+1delinsATG
NM_182776.3:c.191_192+1delinsATG